Component Separator

ABSTRACT

The present invention relates to a component separator capable of guaranteeing the purity of a subject component such as isolated blood or stem cells while simplifying a process compared with a conventional technique, and preventing air contamination during a component separation process, the component separator comprising: a hollow main body having a communication pipe, through which a body fluid communicates, formed at one end portion, and a main body female screw part disposed at the other end portion; a plunger for varying a main body space while moving forward and backward inside the main body; and an operation member having a pressing tube having a pressing male screw part capable of being screwed with the main body female screw part, and a plunger coupling tube having a tube screw screwed with a plunger screw part at the lower part of the plunger by coming into contact with or retracting from the inside of the pressing tube.

FIELD OF THE INVENTION

The present invention relates to a component separator, and morespecifically to a component separator capable of assuring purity ofsubject components such as separated blood or stem cells and preventingcontamination by ambient air during the process of separatingcomponents, while simplifying the processes compared to the related artwith a simple structure.

BACKGROUND OF THE INVENTION

Stem cells are used for various treatments or operation purposes. Inaddition, stem cells may be used for plastic or cosmetic surgery andalso for the treatment of hair loss, chronic and almost incurablediseases, and pain. The scope of utilization of stem cells isconsiderably wide, and it is expected to expand further in the future. Astem cell refers to a cell which has the ability of self-renewal and theability of differentiation into another cells.

Stem cells can be classified largely into embryonic stem cells and adultstem cells. In another way of classification, stem cells can beclassified into autologous cells and allogenic cells. The allogeniccells may include cord blood stem cells, umbilical cord derived stemcells, placenta derived stem cells or the like. The autologous stemcells can be classified largely into bone marrow derived stem cells andadipose derived stem cells (ADSC). The main cells of these arehematopoietic stem cells (HSC) and mesenchymal stem cells (MSC). In aconventional method of separating stem cells, the extraction processprogresses by the application of the extraction method in a laboratory.This process has disadvantages in that the extraction method is veryfastidious, difficult to learn, and takes a lot of time; contaminationcan be caused by air pollution and instruments even due to slightcarelessness in the extraction process; and considerable differences aremade in efficiency by the extracting persons. Because of such reasons,there are needs for easy and simple methods that can also preventcontamination.

The platelet, which is one of the components of blood, contains manytypes of growth factors such as PDGF and TGF-BETA, which are related towound healing. Treatment using these growth factors shows a good effectfor healing skin diseases and wounds. The growth factors in theseplatelets are being used in the form of platelet rich plasma (PRP). Whencentrifugal separation is carried out, most of platelets and white bloodcells are positioned in a buffy coat layer generated on an interfacebetween blood cells and plasma. Furthermore, the plasma (platelet poorplasma (PPP)) in blood is being used for various medical purposes.

Hence, there is still a need for a more convenient and advanced methodfor separating the body fluid components using difference in specificgravity between cells and then extracting each component, for variousmedical purposes.

In particular, in the case of a adipose-derived stem cell, the quantityextracted in comparison with the volume of the whole stock solution (amixed liquid of fat and collagenase solution) is small, so it isdifficult to obtain a high-purity of stem cells by using a conventionalmethod.

Therefore, in order to separate such body fluids, the present applicanthas presented a component separator (Korean Patent Registration No.10-1179548).

However, in the invention of the above patent, due to an external impactmay occur during a separating operation, the separated components may bemixed with each other. Therefore, it is necessary to pay much attentionto the operation when separating only a desired component, which may becumbersome.

See, e.g., Korean Patent Registration No. 10-1179548.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a perspective view of a component separator according to anembodiment of the present invention.

FIG. 2 is an exploded perspective view of the component separatoraccording to the embodiment of the present invention.

FIG. 3 is an exploded perspective view of the component separatoraccording to the embodiment of the present invention when viewing adifferent direction from FIG. 2.

FIG. 4 is a cross-sectional view of the component separator of FIG. 1.

FIG. 5 is a perspective view of the component separator according to theembodiment of the present invention in a state in which an operationmember is removed and a lower plug is inserted.

FIG. 6 is a cross-sectional view illustrating a state in which blood isintroduced in the component separator of FIG. 1.

FIG. 7 is a cross-sectional view illustrating a state in which the bloodintroduced in the component separator of FIG. 6 is separated layer bylayer using a centrifuge.

FIG. 8 is a cross-sectional view illustrating a state in which theoperation member is coupled to the component separator of FIG. 7, andthe operation member is raised and upper blood components of thecomponent separator is pressed so as to supply the component to acomponent collector connected to the component separator.

FIG. 9 is a cross-sectional view of the component separator in a statein which a mixture of pure fat and collagenase solution is separatedlayer by layer using the centrifuge.

FIG. 10 is a cross-sectional view illustrating a state in which theoperation member is coupled to the component separator, and theoperation member is raised and upper supernatant fractions at an upperside is pressed so as to discharge to the component collector.

DETAILED DESCRIPTION Technical Problem

In consideration of the above-mentioned circumstances, it is an objectof the present invention to provide a component separator capable ofassuring purity of a subject component such as separated blood or stemcells and preventing contamination by ambient air during the process ofseparating components, while simplifying the processes compared to therelated art.

Technical Solution

In order to accomplish the foregoing objects, according to an aspect ofthe present invention, there is provided a component separatorincluding: a hollow main body which includes a communication pipe formedat one end portion thereof to allow a flow of body fluids therethroughand a main body female screw part disposed at the other end portion; aplunger which is installed inside of the main body to vary a main bodyspace while moving forward and backward; and an operation member whichincludes a pressing tube having a pressing male screw part to be screwedwith the main body female screw part, and a plunger coupling tube havinga tube screw to be screwed with a plunger screw part formed at a lowerpart of the plunger by slidably moving inside of the pressing tube.

Herein, thread directions of the main body female screw part and thepressing male screw part may be opposite to thread directions of theplunger screw part and the tube screw.

In addition, tube screw may have an offset part formed at an end thereofwithout a thread.

Further, a tube protrusion stopper may be formed at a lower side of thetube screw to limit a protrusion amount of the tube screw.

Further, a tube separation preventing cover may be installed at a lowerside of the pressing tube, and the plunger coupling tube may have a tubeseparation stopper formed at a lower portion of an outer circumferencethereof to limit a movement of the plunger coupling tube.

Further, a spring may be installed between the tube separation stopperand the tube separation preventing cover to easily guide attaching anddetaching of the tube screw with the plunger screw part.

Furthermore, a spring may be installed between a pressing tubeprotrusion formed on the pressing tube and a tube protrusion stopper ofthe plunger coupling tube to easily guide attaching and detaching of thetube screw with the plunger screw part.

Advantageous Effects

According to the present invention, it is possible to reduce the timeand costs required in the separation work of the blood components. Inparticular, due to separating the blood components in an order of PPPand PRP in light specific gravity by pressing upward, it is possible tominimize or prevent mixing of blood cells, thus to reliably assure thepurity of the separated PRP and PPP.

In addition, since the blood component moves in a state isolated fromexternal air during a process of obtaining blood to a process ofseparating the blood components, it is possible to prevent contaminationby the air. Accordingly, it is possible to prevent infection ofpathogens or an occurrence of complications that may occur due to aircontamination of blood in the blood separation process.

Further, separation of the stem cells may be achieved through thecomponent separator of the present invention. In order to separate avery small quantity compared with the stock solution, the operationmember is adopted so as to be able to extract high-purity stem cells ina simple manner. The operation member of a specific form allow a user toeasily extract the stem cells. Thus, the costs of treatments can bereduced drastically in treatments using stem cells.

EXAMPLES

Hereinafter, exemplary embodiments of the present invention will bedescribed in detail with reference to the accompanying drawings.Referring to the drawings, wherein like reference characters designatelike or corresponding parts throughout the several views. In theembodiments of the present invention, a detailed description of publiclyknown functions and configurations that are judged to be able to makethe purport of the present invention unnecessarily obscure are omitted.

FIGS. 1 to 3 illustrate a component separator 100 according to anembodiment of the present invention. The component separator 100basically includes a hollow main body 102 which has a communication pipe108 formed at one end portion thereof to allow a flow of body fluidstherethrough and a main body female screw part 142 disposed at the otherend portion thereof, a plunger 118 which is installed inside of the mainbody 102 to vary a main body space 103 while moving forward and backwardinside of the main body 102, and an operation member which pushes up theplunger 118 and pulls the plunger 118 according to circumstances.

It is preferable that the main body 102 is made of a transparentmaterial so as to view inside thereof, and may be made of plastic orglass. The main body may be connected to other syringes through thecommunication pipe 108 or a communication pipe plug 112 may be coupledthereto.

The main body female screw part 142 is disposed at the other end of themain body 102. The main body female screw part 142 may be integrallyformed with the main body 102, or as illustrated in the embodiment ofthe present invention, the main body female screw part 142 may be formedon a main body cover 138 attached and detached to and from the main body102. The main body cover 138 detachably coupled with the main body 102by a main body cover screw 140 which is screwed to a main body couplingscrew 110 formed at a lower portion of the main body 102.

The main body female screw part 142 may be formed in a continuousthread, but as illustrated in FIGS. 2 and 3, may be formed in aprotrusion form which is a portion of the thread.

The main body 102 has a main body stopper 104 formed on an outercircumference thereof, and is installed in an annular main body adapter114 having an adapter space 115 in which the main body 102 is insertedfrom the communication pipe 108 side to the main body stopper 104. Themain body adapter 114 is installed in order to reduce a tolerance anddecrease a shake thereof, when the component separator 100 is insertedinto a bucket of a centrifuge (not illustrated).

The main body adapter 114 has a scale 116 formed thereon, such that avolume of a material inside the main body 102 may be measured. Further,the main body adapter 114 has a coupling groove 117 formed on a sidethereof The coupling groove 117 is coupled with a coupling protrusion106 formed on an outer circumference of the main body 102 by protrudingtherefrom. As a result, the main body adapter 114 may be placed on themain body 102.

The plunger 118 may vary a space into which body fluids, etc. areintroduced inside the main body 102 while moving forward and backwardinside of the main body 102. A rotational movement of the operationmember is converted into a linear movement of the plunger 118.Accordingly, liquids such as body fluids may be introduced or dischargedbetween the plunger 118 and the communication pipe 108.

In addition, as illustrated in FIGS. 2 and 4, a collection partcontacting with blood or body fluids may be concavely formed on an uppersurface of a plunger head 124 of the plunger 118. Further, a plungerscrew part 126 is formed in a center of a plunger lower portion 122which is integrally formed with the plunger head 124. The plunger screwpart 126 is screwed with a tube screw 148.

The operation member includes a pressing tube 128 having a pressing malescrew part 130 that can be screwed with the main body female screw part142, and a plunger coupling tube 144 which is screwed with the plungerscrew part 126 formed at a lower part of the plunger by slidably movinginside of the pressing tube 128.

The pressing tube 128 has the pressing male screw part 130 formed on theouter circumference thereof and a pressing tube hole 136 formed in anupper portion thereof, into which the tube screw 148 of the plungercoupling tube 144 is inserted. A pressing tube protrusion 132 isdisposed at a front end of the pressing male screw part 130 so as tocontact with a bottom of the plunger lower portion 122. In addition, acover coupling screw 134 may be formed at a rear end of the pressingtube 128 so as to be coupled with a tube separation preventing cover160. Further, the spring may be installed between the pressing tubeprotrusion 132 of the pressing tube 128 and a tube protrusion stopper150 of the plunger coupling tube 144.

The tube screw 148 capable of protruding through the pressing tube hole136 is formed at a tip of the plunger coupling tube 144. The tube screw148 is screwed with the plunger screw part 126. In addition, an offsetpart 152 having a size the same as or smaller than an inner diameter ofthe plunger screw part 126 is formed at the tip of the tube screw 148,so as to limit the movement of the plunger coupling tube 144 byinserting into the plunger screw part 126. It is preferable that theoffset part 152 formed at the upper side of the tube screw 148 protrudesupward from the pressing tube protrusion 132 formed at the tip of thepressing tube 128 in a state in which the tube screw 148 is not screwedwith the plunger screw part 126. That is, when moving forward theplunger 118 by rotating the pressing tube 128, the plunger operates in astate in which only the offset part 152 is simply inserted into theplunger lower portion 122 while being prevented a movement in acircumferential direction.

In addition, it is preferable that thread directions of the main bodyfemale screw part 142 and the pressing male screw part 130 are formed asopposite to thread directions of the plunger screw part 126 and the tubescrew 148. For example, as illustrated in FIG. 2, it is preferable thatthe thread directions of the main body female screw part 142 and thepressing male screw part 130 are formed in a right-hand threaddirection, the thread directions of the plunger screw part 126 and thetube screw 148 are formed in a left-hand thread direction. The reason isthat, if it is necessary to push up the plunger 118 using the pressingtube 128, this operation may be performed in a state in which theplunger screw part 126 and the tube screw 148 are not screwed with eachother. However, if it is necessary to pull the plunger 118 to movebackward, this operation may be performed in only a state in which theplunger screw part 126 and the tube screw 148 are screwed with eachother. Therefore, due to the thread directions formed as opposite toeach other, when moving the plunger 118 backward, the coupling statebetween the plunger screw part 126 and the tube screw 148 may bemaintained while preventing disengaging thereof.

In addition, in order to limit a protrusion amount of the tube screw148, a tube protrusion stopper 150 is formed at a lower side of the tubescrew 148 of a plunger coupling tube body 146. The tube protrusionstopper 150 may be formed in a loop or a protrusion shape.

A tube separation preventing cover 160 is installed at a lower side ofthe pressing tube 128 having a tube separation preventing cover hole 162through which a portion of the plunger coupling tube 144 can penetrate.The plunger coupling tube 144 has a tube separation stopper 154, whosemovement is limited by the tube separation preventing cover 160, formedon a lower portion of the outer circumference thereof at the lower sidefrom the tube protrusion stopper 150. Further, in order to minimize theshake, it is preferable that outer diameters of the tube protrusionstopper 150 and the tube separation stopper 154 are the same as orslightly smaller than the inner diameter of the pressing tube hole 136,thereby reducing the tolerance thereof.

In addition, the plunger coupling tube 144 has a tube gripper 156subjected to knurling processing at the lower portion thereof so as tofacilitate rotation thereof while gripping by a hand.

A spring 158 is installed between the tube separation stopper 154 andthe tube separation preventing cover 160, so as to easily guideattaching and detaching of the tube screw 148 with the plunger screwpart 126. One end of the spring 158 is in contact with the tubeseparation stopper 154, and the other end thereof is seated on a springseat 164 formed in the tube separation preventing cover 160. Further,both ends of the spring 158 may be directly coupled with the tubeseparation stopper 154 and the spring seat 164 of the tube separationpreventing cover 160.

The component separator 100 according to the first embodiment of thepresent invention basically has the above described configuration.Hereinafter, a process for separating components using the componentseparator 100 will be described.

First, a process for separating blood components into PPP and PRP willbe described. Plasma 4 containing a buffy coat layer 3 is referred to asa platelet rich plasma (PRP), and plasma 4 not containing the buffy coatlayer 3 is referred to as a platelet poor plasma (PPP). First, blood 1is introduced in the component separator 100 using a syringe 10, asillustrated in FIG. 6. If the component separator 100 containing theintroduced blood 1 is centrifuged with being clogged by thecommunication pipe plug 112, the blood components are divided into bloodcells 2, the buffy coat layer 3, and the plasma 4 layer by layer fromthe bottom layer. In this state, when performing the centrifuge, asillustrated in FIG. 5, it is possible to prevent contamination byclogging the lower portion of the main body 102 by a main body plug 170.A main body plug coupling member 172 is formed in the main body plug170, such that the main body plug may be stably coupled to the lowerportion of the main body 102.

Next, the communication pipe plug 112 is removed, and another syringe 20is connected to the communication pipe 108, then the operation member iscoupled to the lower portion of the main body 102. Thereafter, whenrotating the pressing tube 128, the main body female screw part 142 andthe pressing male screw part 130 are screwed with each other, andthereby the plunger 118 is raised while the pressing tube 128 is raised.In this case, the thread directions of the plunger screw part 126 andthe tube screw 148 are opposite to the thread directions of the mainbody female screw part 142 and the pressing male screw part 130, anunscrewed state is maintained. In addition, the offset part 152 isinserted into the plunger screw part 126, such that a rotation center ofthe plunger screw part 126 and a rotation center of the plunger couplingtube 144 may coincide with each other while the plunger coupling tube144 is not shaken.

As a result, the components to be separated such as the plasma 4 may bedischarged toward the syringe 20. Thereafter, the above-described workmay be repeatedly performed to separate a higher purity component.

Next, a method of separating adipose-derived stem cells will bedescribed. First, in order to extract adipose-derived stem cells, fatsare obtained by a method such as suction. Then, water portion is removedfrom the obtained fats through a decanting process or centrifugationprocess to obtain pure fats. Thereafter, collagenase solution in whichsaline water and collagenase are blended, is mixed in the obtained purefats. Additionally, an incubation process in which stem cells existingbetween fat cells are allowed to be liberated sufficiently is carriedout.

Then, a subject solution containing the stem cells introduced into thecomponent separator 100 through the communication pipe 108.Alternatively, after the pure fats and the collagenase solution aremixed, the mixture is directly introduced into the component separator100, thereby the incubation process for liberating the stem cellsexisting between fat cells may be carried out in the component separator100.

Then, the component separator 100 is inserted into a syringe (notillustrated) to separate the subject solution layer by layer.Consequently, as illustrated in FIG. 9, a stem cell fraction solution 5is arranged at the lower side, and a supernatant fraction 6 is arrangedat the upper side. (Strictly speaking, a mass in which cells present ina pellet form are concentrated in a collection part 120 may refer to astem cell fraction, and a state in which the stem cell fraction isfloated on a small amount of the supernatant fraction 6 may refer to astem cell fraction solution, for convenience of explanation, both of thestem cell fraction and a stem cell fraction solution refer to as a stemcell fraction solution). Next, as illustrated in FIG. 10, most of thesupernatant fraction 6 is discharged using the operation member, andonly the supernatant fraction 5 remains at the lower side.

Further, a cleaning liquid is again supplied in the component separator100. In this case, another syringe is connected to the communicationpipe 108, then the cleaning liquid is introduced into the main body 102by pressing the syringe, or an upper syringe containing the cleaningliquid is connected to the communication pipe 108, then the cleaningliquid may be introduced by a method of moving the operation memberbackward. In this case, the plunger 118 is moved backward both byrotating the plunger coupling tube 144 to couple the plunger screw part126 with the tube screw 148 and by rotating the pressing tube 128,

Since the tube screw 148 and the pressing male screw part 130 havethread directions opposite to each other, even if the pressing tube 128is rotated, the coupling state between the plunger screw part 126 andthe tube screw 148 is maintained. Then, the component separator 100containing the additionally introduced cleaning liquid is again mountedin the centrifuge, the layer separation process is performed. Byrepeatedly performing the above-described processes, a desired stem cellfraction solution may be finally obtained.

Next, a method of separating bone marrow-derived stem cells will bedescribed. In the case of the bone marrow-derived stem cells, at first,bone marrow is extracted from portions such as iliac bone using aspecial needle for bone marrow extraction. Since bone marrow extract hasan appearance similar to blood, it can be extracted by a methodidentical to the blood component separation method described above.

Furthermore, by using the above-described method, lymphoid cells, immunecells, cord blood stems cells, etc. can also be separated by usingdifferences in specific gravity. That is, autologous/allogenic cells orxenogeneic cells can be separated also by using the above method inwhich differences in specific gravity of cells are used.

Although the present invention has been described in connection with theexemplary embodiments illustrated in the drawings, it is onlyillustrative. It will be understood by those skilled in the art thatvarious modifications and equivalents can be made to the presentinvention. Therefore, the true technical scope of the present inventionshould not be defined by the appended claims.

Description of Reference Numerals 1: blood 2: blood cell 3: buffy coatlayer 4: plasma 5: stem cell fraction solution 6: supernatant fraction10, 20: syringe 12, 22: syringe plunger 100: component separator 102:main body 103: main body space 104: main body stopper 106: couplingprotrusion 108: communication pipe 110: main body coupling screw 112:communication pipe plug 114; main body adapter 115: adapter space 116:scale 117: coupling groove 118: plunger 120: collection part 122:plunger lower portion 124: plunger head 126: plunger screw part 128:pressing tube 130: pressing male screw part 132: pressing tubeprotrusion 134: cover coupling screw 136: pressing tube hole 138: mainbody cover 140: main body cover screw 142: main body female screw part144: plunger coupling tube 146: plunger coupling tube body 148: tubescrew 150: tube protrusion stopper 152: offset part 154: tube separationstopper 156: tube gripper 158: spring 160: tube separation preventingcover 162: tube separation preventing 164: spring seat cover hole 170:main body plug 172: main body plug coupling member

1. A component separator comprising: a hollow main body which includes acommunication pipe formed at one end portion thereof to allow a flow ofbody fluids therethrough and a main body female screw part disposed atthe other end portion; a plunger which is installed inside of the mainbody to vary a main body space while moving forward and backward; and anoperation member which includes a pressing tube having a pressing malescrew part to be screwed with the main body female screw part, and aplunger coupling tube having a tube screw to be screwed with a plungerscrew part formed at a lower part of the plunger by slidably movinginside of the pressing tube.
 2. The component separator according toclaim 1, wherein thread directions of the main body female screw partand the pressing male screw part are opposite to thread directions ofthe plunger screw part and the tube screw.
 3. The component separatoraccording to claim 1, wherein the tube screw has an offset part formedat an end thereof without a thread.
 4. The component separator accordingto claim 1, wherein a tube protrusion stopper is formed at a lower sideof the tube screw to limit a protrusion amount of the tube screw.
 5. Thecomponent separator according to claim 1, wherein a tube separationpreventing cover is installed at a lower side of the pressing tube, andthe plunger coupling tube has a tube separation stopper formed at alower portion of an outer circumference thereof to limit a movement ofthe plunger coupling tube.
 6. The component separator according to claim5, wherein a spring is installed between the tube separation stopper andthe tube separation preventing cover to easily guide attaching anddetaching of the tube screw with the plunger screw part.
 7. Thecomponent separator according to claim 5, wherein a spring is installedbetween a pressing tube protrusion formed on the pressing tube and atube protrusion stopper of the plunger coupling tube to easily guideattaching and detaching of the tube screw with the plunger screw part.